1,2-diacetals: a new opportunity for organic synthesis.
The use of 1,2-diacetals for a number of synthetic applications to provide diol protection and reactivity control was studied. The chiral versions of these systems were used to desymmetrize the enantiotopic diol pairs and to discriminate diequatorial diols in many carbohydrate derivatives. The fusio...
Главные авторы: | Ley, S, Baeschlin, D, Dixon, D, Foster, A, Ince, S, Priepke, H, Reynolds, D |
---|---|
Формат: | Journal article |
Язык: | English |
Опубликовано: |
ACS
2001
|
Схожие документы
-
A general and efficient procedure for the preparation of enantiopure anti-1,2-diols - synthesis and utility of (R ',R ',S,R)-2,3-butane diacetal protected butane tetrol
по: Dixon, D, и др.
Опубликовано: (1999) -
Preparation of desymmetrised meso-tartrate derivatives - synthesis and utility of (R ',R ',R,S)-2,3-butane diacetal protected dimethyl tartrate
по: Dixon, D, и др.
Опубликовано: (1999) -
New building blocks for efficient and highly diastereoselective polyol production - Synthesis and utility of (R ',R ',S,S) and (S ',S ',R,R)-2,3-butane diacetal protected butane tetrol derivatives
по: Barlow, J, и др.
Опубликовано: (1999) -
The total synthesis of (+)-aspicilin using 2,3-butane diacetal protected butane tetrols via a chiral memory protocol
по: Dixon, D, и др.
Опубликовано: (2001) -
Butane-2,3-diacetal-desymmetrized glycolic acid—a new building block for the stereoselective synthesis of enantiopure α-hydroxy acids
по: Díez, E, и др.
Опубликовано: (2001)